Canonical Allele Identifier: CA1148236142

Gene: HSPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21865798G= , CM000663.2:g.21865798G=	GRCh38
NC_000001.10:g.22192291G= , CM000663.1:g.22192291G=	GRCh37
NC_000001.9:g.22064878G=	NCBI36
NG_016740.1:g.76460C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.4233C= MANE Select	ENSP00000363827.3:p.Tyr1411=
ENST00000644714.1:c.627C=	ENSP00000496473.1:p.Tyr209=
ENST00000374695.7:c.4233C=	ENSP00000363827.3:p.Tyr1411=
NM_001291860.1:c.4236C=	NP_001278789.1:p.Tyr1412=
NM_005529.6:c.4233C=	NP_005520.4:p.Tyr1411=
XM_006710594.2:c.4779C=	XP_006710657.1:p.Tyr1593=
XM_006710595.2:c.4731C=	XP_006710658.1:p.Tyr1577=
XM_006710596.2:c.4710C=	XP_006710659.1:p.Tyr1570=
XM_006710597.2:c.4233C=	XP_006710660.1:p.Tyr1411=
XM_011541317.1:c.4782C=	XP_011539619.1:p.Tyr1594=
XM_011541318.1:c.4782C=	XP_011539620.1:p.Tyr1594=
XM_011541319.1:c.4782C=	XP_011539621.1:p.Tyr1594=
XM_011541320.1:c.4782C=	XP_011539622.1:p.Tyr1594=
XM_011541321.1:c.4287C=	XP_011539623.1:p.Tyr1429=
XM_011541322.1:c.4782C=	XP_011539624.1:p.Tyr1594=
XM_011541318.2:c.4782C=	XP_011539620.1:p.Tyr1594=
XM_017001120.1:c.4428C=	XP_016856609.1:p.Tyr1476=
XM_017001121.1:c.4377C=	XP_016856610.1:p.Tyr1459=
XM_017001122.1:c.4374C=	XP_016856611.1:p.Tyr1458=
NM_005529.7:c.4233C= MANE Select	NP_005520.4:p.Tyr1411=
NM_001291860.2:c.4236C=	NP_001278789.1:p.Tyr1412=